Oligophrenin 1

Preferred Label : Oligophrenin 1;

Symbol : OPHN1;

CISMeF acronym : OPHN1;

Type : Gene;

Alternative titles and symbols : OPN1;

Ensembl ID : ENSG00000079482;

Prefixed ID : *300127;

Details

Origin ID

300127;

UMLS CUI

C1417960;

Automatic exact mappings (from CISMeF team)
- OPHN1 Gene [NCIt concept]
- OPHN1 wt Allele [NCIt concept]
- Oligophrenin-1 [NCIt concept]
- oligophrenin 1 [ORDO Gene]
- oligophrenin 1 [HGNC gene]
HGNC gene
- oligophrenin 1 [HGNC gene]
NCIt concept(s)
- OPHN1 Gene [NCIt concept]
- OPHN1 wt Allele [NCIt concept]
- Oligophrenin-1 [NCIt concept]
ORDO concept(s)
- oligophrenin 1 [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder, X-linked, syndromic, billuart type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- OPHN1 Gene [NCIt concept]
- oligophrenin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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